| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219178142-219178354 | Common:6; Rare:111 | ||||
| chr2:219206683-219206923 | Rare:87 | ||||
| chr2:219229342-219229398 | Rare:19 | ||||
| chr2:219229548-219229905 | Common:2; Rare:115 | ||||
| chr2:219245416-219245511 | Rare:24 | ||||
| chr2:219253884-219254056 | Common:1; Rare:54 | ||||
| chr2:219387327-219387435 | Common:1; Rare:22 | ||||
| chr2:219418362-219419080 | Common:6; Rare:234; Clinvar:40; Clinvar (benign):24; Clinvar (pathogenic):3 | ||||
| chr2:219419845-219420173 | Common:2; Rare:68; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr2:219420237-219420656 | Common:4; Rare:123; Clinvar:18; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr2:219437155-219437451 | Common:1; Rare:51 | ||||
| chr2:219441905-219442073 | Rare:38 | ||||
| chr2:219451544-219451642 | Common:1; Rare:28 | ||||
| chr2:219460558-219460949 | Common:3; Rare:82 | ||||
| chr2:219461289-219461446 | Rare:35 |